Canonical Allele Identifier: CA394811579

Gene: ERCC4

Linked Data

• dbSNP Id: rs2141607663
• MyVariant Identifiers: chr16:g.14029354C>A (hg19) ; chr16:g.13935497C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935497C>A , CM000678.2:g.13935497C>A	GRCh38
NC_000016.9:g.14029354C>A , CM000678.1:g.14029354C>A	GRCh37
NC_000016.8:g.13936855C>A	NCBI36
NG_011442.1:g.20341C>A , LRG_463:g.20341C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1643C>A
ENST00000682617.1:c.1703C>A	ENSP00000507912.1:p.Pro568Gln
ENST00000682826.1:c.*879C>A	ENSP00000507274.1:n.*879C>A
ENST00000682909.1:n.3605C>A
ENST00000683277.1:n.3210C>A
ENST00000683407.1:n.1573C>A
ENST00000683962.1:c.*1259C>A	ENSP00000506854.1:n.*1259C>A
ENST00000311895.8:c.1565C>A MANE Select	ENSP00000310520.7:p.Pro522Gln
ENST00000311895.7:c.1565C>A	ENSP00000310520.7:p.Pro522Gln
ENST00000389138.7:n.842C>A
NM_005236.2:c.1565C>A , LRG_463t1:c.1565C>A	NP_005227.1:p.Pro522Gln
XM_011522424.1:c.1703C>A	XP_011520726.1:p.Pro568Gln
XM_011522425.1:c.1022C>A	XP_011520727.1:p.Pro341Gln
XM_011522426.1:c.776C>A	XP_011520728.1:p.Pro259Gln
XM_011522427.1:c.215C>A	XP_011520729.1:p.Pro72Gln
XR_932805.1:n.1724C>A
XM_011522424.3:c.1703C>A	XP_011520726.1:p.Pro568Gln
XM_017023043.2:c.776C>A	XP_016878532.1:p.Pro259Gln
NM_005236.3:c.1565C>A MANE Select	NP_005227.1:p.Pro522Gln